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Dehydroemetine

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20 with metronidazole. One-fourth of the patients treated with dehydroemetine reported adverse reactions, compared to 20% with other drugs, but no patient discontinued therapy due to the reaction. In all three cases, the drug therapy resulted in clearance of the infection, defined as negative results through an O&P exam, in all but 1-2 patients.
561:, a condition which can produce painful neurological symptoms. The study involved 40 patients, all of whom were over 60, and compared dehydroemetine treatment to another drug. The study reported patients treated with dehydroemetine experienced relief of neuralgia with no changes in cardiovascular functions. 522:
A double-blind study of oral dehydroemetine in the treatment of amoebiasis performed at St. Mary's Hospital, Catholic Medical College, Seoul, Republic of Korea in 1973-1974 showed dehydroemetine treatment was effective. A total of 60 patients were treated, 20 with dehydroemetine, 20 with Tiberal, and
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in its anti-amoebic properties and structure (they differ only in a double bond next to the ethyl substituent), but it produces fewer side effects. In the United States, it is manufactured by
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Chintana T, Sucharit P, Mahakittikun V, Siripanth C, Suphadtanaphongs W (December 1986). "In vitro studies on the sensitivity of local Entamoeba histolytica to anti-amoebic drugs".
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InChI=1S/C29H38N2O4/c1-6-18-17-31-10-8-20-14-27(33-3)29(35-5)16-23(20)25(31)12-21(18)11-24-22-15-28(34-4)26(32-2)13-19(22)7-9-30-24/h13-16,24-25,30H,6-12,17H2,1-5H3/t24-,25+/m1/s1
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A 1979 study of 27 patients treated with dehydroemetine and various other drugs suggested all drug combinations were successful at treating amoebic liver abscesses.
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Peters M, Dietrich M, Bienzle U, Kern P, Mannweiler E (December 1979). "Amoebic liver abscess: a retrospective clinical evaluation of twenty-seven cases".
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Al-Khateeb GH, Al-Jeboori TI, Al-Janabi KA (1977). "In vitro efficacy of some drugs on promastigotes of Leishmania donovani".
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Hernandez-Perez E (April 1980). "Dehydroemetine therapy for herpes zoster. A comparison with corticosteroids".
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A 1986 in vitro study compared the effects of dehydroemetine, metronidazole, ornidazole, and secnidazole on
301: 182: 1235: 262: 251: 537:. Metronidazole was found to be most effective, and the other three drugs were of similar effectiveness. 488: 764:
Panwar P, Burusco KK, Abubaker M, Matthews H, Gutnov A, FernĂĄndez-Álvaro E, et al. (March 2020).
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Some examples of the use of dehydroemetine in the treatment of amoebic infections include:
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Magaña-García M, Arista-Viveros A (December 1993). "Cutaneous amebiasis in children".
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in a 7-year-old girl with dehydroemetine and metronidazole in Mexico.
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The Southeast Asian Journal of Tropical Medicine and Public Health
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A 1980 report described the use of dehydroemetine in treatment of
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O(c1cc2c(cc1OC)(NCC2)CC\5=C(/CC)CN4(c3c(cc(OC)c(OC)c3)CC4)C/5)C
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Dehydroemetine has been investigated as a treatment for
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It was at one-time, but is no longer distributed by the
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Handbook of drugs for tropical parasitic infections
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503:-resistant amoebiasis. 482: 1307:Isoquinoline alkaloids 1063:Diiodohydroxyquinoline 638:Pediatric Dermatology 534:Entamoeba histolytica 499:for the treatment of 1317:Norsalsolinol ethers 1312:Antiprotozoal agents 908:antiprotozoal agents 783:10.1128/AAC.01444-19 497:investigational drug 517:cutaneous amebiasis 455:antiprotozoal agent 108:-pyridoisoquinoline 23: 1284:Never to phase III 1025:Luminal amebicides 618:on 9 February 2006 507:Amoebic infections 19: 1294: 1293: 1230: 1229: 1140: 1139: 1090:Dichloroacetamide 1019: 1018: 938:Tissue amebicides 856:10.1159/000221994 542:In other diseases 493:compassionate use 448: 447: 376:Interactive image 263:CompTox Dashboard 16:Chemical compound 1324: 1034:Hydroxyquinoline 1030: 1029: 943: 942: 934: 933: 897: 890: 883: 874: 873: 868: 867: 839: 833: 832: 812: 806: 805: 795: 785: 776:(4). e01444-19. 761: 755: 754: 734: 728: 727: 707: 701: 700: 698: 696: 676: 670: 669: 633: 627: 626: 624: 623: 608: 602: 601: 586:Abdi YA (1995). 583: 444: 443: 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Retrieved 688: 684: 674: 641: 637: 631: 620:. Retrieved 616:the original 606: 587: 581: 565: 563: 556: 547: 545: 532: 510: 495:basis as an 486: 474: 472: 450: 449: 438:   432:   252:ChEMBL547470 105: 101: 1270:from market 1244:Propamidine 1197:quinazoline 1181:Phanquinone 1166:Difetarsone 1132:Paromomycin 1092:derivatives 1036:derivatives 981:Azanidazole 976:Secnidazole 949:derivatives 695:November 9, 570:infection. 457:similar to 359: g·mol 302:100.023.220 84:Identifiers 1301:Categories 1221:Fumagillin 1161:Carbarsone 1099:Diloxanide 1070:Clioquinol 971:Nimorazole 966:Ornidazole 961:Tinidazole 622:2007-09-09 574:References 567:Leishmania 364:3D model ( 352:Molar mass 232:CHEBI:4363 192:7S79QT1T91 163:ChemSpider 118:CAS Number 93:IUPAC name 1280:Phase III 1268:Withdrawn 1191:Mepacrine 1156:Arsthinol 1109:Etofamide 1104:Clefamide 1080:Chiniofon 1078:related: 929:Entamoeba 916:amebicide 912:amoebozoa 469:Mechanism 127:4914-30-1 46:Drugs.com 1207:thiazole 1114:Teclozan 906: â€“ 802:31964796 666:41438097 548:in-vitro 476:in vitro 441:(verify) 60:ATC code 1152:arsenic 1068:I, Cl ( 1006:Emetine 829:6102504 793:7179302 751:2883732 658:8302738 552:malaria 546:A 2020 459:emetine 357:478.633 319:Formula 138:PubChem 76:) 70: ( 68:P01AX09 1263:WHO-EM 862:  827:  800:  790:  749:  724:538815 722:  664:  656:  594:  390:SMILES 243:ChEMBL 212:D00828 995:Other 864:16732 817:Cutis 662:S2CID 491:on a 463:Roche 410:InChI 366:JSmol 223:ChEBI 172:19773 152:21022 1049:Br ( 1042:Cl ( 860:PMID 825:PMID 798:PMID 747:PMID 720:PMID 697:2015 654:PMID 592:ISBN 483:Uses 203:KEGG 183:UNII 100:(11b 42:AHFS 1061:I ( 920:P01 852:doi 788:PMC 778:doi 646:doi 268:EPA 142:CID 73:WHO 1303:: 1276:: 858:. 848:23 846:. 821:25 819:. 796:. 786:. 774:64 772:. 768:. 743:17 741:. 716:30 714:. 687:. 683:. 660:. 652:. 642:10 640:. 554:. 465:. 333:38 327:29 1223:) 1219:( 1213:) 1209:( 1203:) 1199:( 1193:) 1189:( 1183:) 1179:( 1173:) 1154:( 1072:) 1065:) 1058:) 1046:) 1012:) 1008:/ 1004:( 922:) 918:( 914:/ 896:e 889:t 882:v 866:. 854:: 831:. 804:. 780:: 753:. 726:. 699:. 689:6 668:. 648:: 625:. 600:. 368:) 345:4 342:O 339:2 336:N 330:H 324:C 270:) 266:( 106:H 102:S 44:/

Index


AHFS
Drugs.com
International Drug Names
ATC code
P01AX09
WHO
IUPAC name
CAS Number
4914-30-1
PubChem
21022
ChemSpider
19773
UNII
7S79QT1T91
KEGG
D00828
ChEBI
CHEBI:4363
ChEMBL
ChEMBL547470
CompTox Dashboard
DTXSID901023600
Edit this at Wikidata
ECHA InfoCard
100.023.220
Edit this at Wikidata
Formula
Molar mass

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